Category:Name reactions
From Infogalactic: the planetary knowledge core
A name reaction is a chemical reaction named after its discoverers or developers.
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Pages in category "Name reactions"
The following 200 pages are in this category, out of 289 total.
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B
- Baeyer–Drewson indigo synthesis
- Baker–Venkataraman rearrangement
- Bamberger rearrangement
- Bamford–Stevens reaction
- Bardhan–Senguph phenanthrene synthesis
- Bartoli indole synthesis
- Barton–Kellogg reaction
- Barton–McCombie deoxygenation
- Barton–Zard reaction
- Bechamp reaction
- Bechamp reduction
- Beckmann rearrangement
- Belousov–Zhabotinsky reaction
- Benkeser reaction
- Bergman cyclization
- Bergmann azlactone peptide synthesis
- Bergmann degradation
- Bernthsen acridine synthesis
- Betti reaction
- Biginelli reaction
- Bingel reaction
- Birch reduction
- Birkeland–Eyde process
- Bischler–Napieralski reaction
- Blaise ketone synthesis
- Blanc chloromethylation
- Borodin reaction
- Bosch reaction
- Boudouard reaction
- Boyland–Sims oxidation
- Bray–Liebhafsky reaction
- Briggs–Rauscher reaction
- Brook rearrangement
- Bucherer carbazole synthesis
- Buchwald–Hartwig amination
C
- Camps quinoline synthesis
- Cannizzaro reaction
- Carroll rearrangement
- Castro–Stephens coupling
- Chan rearrangement
- Claisen rearrangement
- Combes quinoline synthesis
- Cook–Heilbron thiazole synthesis
- Cope reaction
- Cope rearrangement
- Corey-Chaykovsky reagent
- Corey–Fuchs reaction
- Corey–Kim oxidation
- Creighton process
- Curtius rearrangement
D
- Dakin oxidation
- Dakin–West reaction
- Darzens reaction
- Davis–Beirut reaction
- DeMayo reaction
- Demjanov rearrangement
- Dess–Martin periodinane
- Devarda's alloy
- Dieckmann condensation
- Diels–Alder reaction
- Dimroth rearrangement
- Doebner reaction
- Doebner–Miller reaction
- Wulff–Dötz reaction
- Dowd–Beckwith ring-expansion reaction
- Duff reaction
E
F
- Favorskii rearrangement
- Feist–Benary synthesis
- Ferrier rearrangement
- Finkelstein reaction
- Fischer–Speier esterification
- Fischer glycosidation
- Fischer indole synthesis
- Fischer oxazole synthesis
- Fleming–Tamao oxidation
- Formose reaction
- Forster–Decker method
- Friedel–Crafts reaction
- Friedländer synthesis
- Fries rearrangement
- Fujimoto–Belleau reaction
- Fukuyama coupling
- Fukuyama reduction
G
H
- Haber–Weiss reaction
- Hajos–Parrish–Eder–Sauer–Wiechert reaction
- Hammick reaction
- Hantzsch pyridine synthesis
- Haworth Phenanthrene synthesis
- Hayashi rearrangement
- Heck reaction
- Hell–Volhard–Zelinsky halogenation
- Hoesch reaction
- Hofmann elimination
- Hofmann rearrangement
- Hofmann–Löffler reaction
- Hooker reaction
- Horner–Wadsworth–Emmons reaction
- Hunsdiecker reaction
I
K
L
M
- Maillard reaction
- Mannich reaction
- Markó–Lam deoxygenation
- Marschalk reaction
- Marsh test
- McLafferty rearrangement
- McMurry reaction
- Meerwein arylation
- Menshutkin reaction
- Meyer synthesis
- Meyer–Schuster rearrangement
- Meyers synthesis
- Michael reaction
- Michaelis–Arbuzov reaction
- Milas hydroxylation
- Mitsunobu reaction
- Mukaiyama aldol addition
- Mumm rearrangement
N
P
- Paal–Knorr synthesis
- Passerini reaction
- Perkin reaction
- Perkow reaction
- Petasis reaction
- Peterson olefination
- Petrenko-Kritschenko piperidone synthesis
- Pfitzinger reaction
- Pfitzner–Moffatt oxidation
- Pictet–Hubert reaction
- Pictet–Spengler reaction
- Pinner reaction
- Povarov reaction
- Prato reaction
- Prins reaction
- Pummerer rearrangement
